Biochip and target DNA quantitative method

1. A biochip, comprising: a supply reservoir: a waste chamber: a first group of chambers, each chamber of the first group of chambers including: a type I chamber including: a primer that is designed to bind to the target DNA; an internal standard DNA of a first amount that has a sequence different from a sequence of the target DNA, and is amplifiable with the primer; and a fluorescent probe that is designed to bind to a part of a PCR product of the target DNA and to a part of a PCR product of the internal standard DNA, and fluoresces differently for the PCR product of the target DNA and the PCR product of the internal standard DNA, and a type II chamber including; the internal standard DNA of a second amount different from the first amount; the primer; and the fluorescent probe, wherein the supply reservoir, the waste chamber, and each of the type I and type II chambers are formed between a first substrate and a second substrate, and the supply reservoir, each of the type I chambers and the type II chambers, and the waste chamber define a plurality of pathways formed between the first substrate and the second substrate; and wherein the plurality of pathways are configured such that in a first orientation the plurality of pathways prevent a reaction mixture of the primers, the fluorescent probes, and the internal standard DNAs from flowing to the waste chamber, and in a second orientation the plurality of pathways allow the reaction mixture to flow to the waste chamber.

2. The biochip according to claim 1 , wherein the plurality of pathways include a first path connected to the type I chamber and the type II chamber; and the supply reservoir is connected to the first path.

3. A biochip, comprising: a supply reservoir: a waste chamber: a first group of chambers, each chamber of the first group of chambers including: a first type I chamber including: a first primer that is designed to bind to the target DNA; a first internal standard DNA of a first amount that has a sequence different from a sequence of the target DNA, and is amplifiable with the first primer; and a first fluorescent probe that is designed to bind to a part of a PCR product of the target DNA and to a part of a PCR product of the first internal standard DNA, and fluoresces differently for the PCR product of the target DNA and the PCR product of the first internal standard DNA, and a first type II chamber including: the internal standard DNA of a second amount different from the first amount; the first primer; and the first fluorescent probe, wherein the supply reservoir, the waste chamber, and each of the first type I and first type II chambers are formed between a first substrate and a second substrate, and the supply reservoir, each of the first type I chambers, the first type II chambers, and the waste chamber are connected by a plurality of pathways formed between the first substrate and the second substrate; and a second group of chambers, each chamber of the second group of chambers including: a second type I chamber including: a second primer different from the first primer that is designed to bind to the target DNA; a second internal standard DNA different from the first internal standard DNA of a third amount that has a sequence different from a sequence of the target DNA, and is amplifiable with the second primer; and a second fluorescent probe that is designed to bind to a part of a PCR product of the target DNA and to a part of a PCR product of the second internal standard DNA, and fluoresces differently for the PCR product of the target DNA and the PCR product of the second internal standard DNA, and a second type II chamber including: the second internal standard DNA of a fourth amount different from the third amount; the second primer; and the second fluorescent probe, wherein each of the second type I and second type II chambers are formed between the first substrate and the second substrate, and the supply reservoir, each of the second type I chambers, the second type II chambers, and the waste chamber are connected by another plurality of pathways formed between the first substrate and the second substrate, wherein the plurality of pathways and the another plurality of pathways are each configured such that the plurality of pathways and the another plurality of pathways in a first orientation prevent a reaction mixture of the primers, the fluorescent probes, and the internal standard DNAs from flowing to the waste chamber, and in a second orientation the plurality of pathways and the another plurality of pathways allow the reaction mixture to flow to the waste chamber.